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Early-Onset Alzheimer’s Disease: What Is Missing in Research?

PURPOSE OF REVIEW: Early-onset Alzheimer’s disease (EOAD), defined as Alzheimer’s disease (AD) occurring before age 65, is significantly less well studied than the late-onset form (LOAD) despite EOAD often presenting with a more aggressive disease progression. The aim of this review is to summarize...

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Autores principales: Ayodele, Temitope, Rogaeva, Ekaterina, Kurup, Jiji T., Beecham, Gary, Reitz, Christiane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815616/
https://www.ncbi.nlm.nih.gov/pubmed/33464407
http://dx.doi.org/10.1007/s11910-020-01090-y
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author Ayodele, Temitope
Rogaeva, Ekaterina
Kurup, Jiji T.
Beecham, Gary
Reitz, Christiane
author_facet Ayodele, Temitope
Rogaeva, Ekaterina
Kurup, Jiji T.
Beecham, Gary
Reitz, Christiane
author_sort Ayodele, Temitope
collection PubMed
description PURPOSE OF REVIEW: Early-onset Alzheimer’s disease (EOAD), defined as Alzheimer’s disease (AD) occurring before age 65, is significantly less well studied than the late-onset form (LOAD) despite EOAD often presenting with a more aggressive disease progression. The aim of this review is to summarize the current understanding of the etiology of EOAD, their translation into clinical practice, and to suggest steps to be taken to move our understanding forward. RECENT FINDINGS: EOAD cases make up 5–10% of AD cases but only 10–15% of these cases show known mutations in the APP, PSEN1, and PSEN2, which are linked to EOAD. New data suggests that these unexplained cases following a non-Mendelian pattern of inheritance is potentially caused by a mix of common and newly discovered rare variants. However, only a fraction of this genetic variation has been identified to date leaving the molecular mechanisms underlying this type of AD and their association with clinical, biomarker, and neuropathological changes unclear. SUMMARY: While great advancements have been made in characterizing EOAD, much work is needed to disentangle the molecular mechanisms underlying this type of AD and to identify putative targets for more precise disease screening, diagnosis, prevention, and treatment.
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spelling pubmed-78156162021-01-25 Early-Onset Alzheimer’s Disease: What Is Missing in Research? Ayodele, Temitope Rogaeva, Ekaterina Kurup, Jiji T. Beecham, Gary Reitz, Christiane Curr Neurol Neurosci Rep Dementia (K.S. Marder, Section Editor) PURPOSE OF REVIEW: Early-onset Alzheimer’s disease (EOAD), defined as Alzheimer’s disease (AD) occurring before age 65, is significantly less well studied than the late-onset form (LOAD) despite EOAD often presenting with a more aggressive disease progression. The aim of this review is to summarize the current understanding of the etiology of EOAD, their translation into clinical practice, and to suggest steps to be taken to move our understanding forward. RECENT FINDINGS: EOAD cases make up 5–10% of AD cases but only 10–15% of these cases show known mutations in the APP, PSEN1, and PSEN2, which are linked to EOAD. New data suggests that these unexplained cases following a non-Mendelian pattern of inheritance is potentially caused by a mix of common and newly discovered rare variants. However, only a fraction of this genetic variation has been identified to date leaving the molecular mechanisms underlying this type of AD and their association with clinical, biomarker, and neuropathological changes unclear. SUMMARY: While great advancements have been made in characterizing EOAD, much work is needed to disentangle the molecular mechanisms underlying this type of AD and to identify putative targets for more precise disease screening, diagnosis, prevention, and treatment. Springer US 2021-01-19 2021 /pmc/articles/PMC7815616/ /pubmed/33464407 http://dx.doi.org/10.1007/s11910-020-01090-y Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Dementia (K.S. Marder, Section Editor)
Ayodele, Temitope
Rogaeva, Ekaterina
Kurup, Jiji T.
Beecham, Gary
Reitz, Christiane
Early-Onset Alzheimer’s Disease: What Is Missing in Research?
title Early-Onset Alzheimer’s Disease: What Is Missing in Research?
title_full Early-Onset Alzheimer’s Disease: What Is Missing in Research?
title_fullStr Early-Onset Alzheimer’s Disease: What Is Missing in Research?
title_full_unstemmed Early-Onset Alzheimer’s Disease: What Is Missing in Research?
title_short Early-Onset Alzheimer’s Disease: What Is Missing in Research?
title_sort early-onset alzheimer’s disease: what is missing in research?
topic Dementia (K.S. Marder, Section Editor)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815616/
https://www.ncbi.nlm.nih.gov/pubmed/33464407
http://dx.doi.org/10.1007/s11910-020-01090-y
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